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Osteoarthritis and Cartilage|December 27, 2005
Asporin and knee osteoarthritis in patients of Greek originM Kaliakatsos, M Tzetis, E Kanavakis, et al.
Hemoglobin|November 24, 1999
Hb Aghia Sophia [alpha62(E11)Val-->0 (alpha1)], an "in-frame" deletion causing alpha-thalassemiaJ Traeger-Synodinos, C L Harteveld, E Kanavakis, et al.
Breast (Edinburgh, Scotland)|October 2, 2007
Association of repeat polymorphisms in the estrogen receptors alpha, beta (ESR1, ESR2) and androgen receptor (AR) genes with the occurrence of breast cancerA Tsezou, M Tzetis, C Gennatas, et al.
Neuromuscular Disorders : NMD|February 24, 2012
Mutation spectrum and phenotypic manifestation in FSHD Greek patientsP Sakellariou, K Kekou, H Fryssira, et al.
Hemoglobin|November 24, 1999
Interaction of an alpha(+)-thalassemia deletion with either a highly unstable alpha-globin variant (alpha2, codon 59, GGC-->GAC) or a nondeletional alpha-thalassemia mutation (AATAAA-->AATAAG): comparison of phenotypes illustrating "dominant" alpha-thalassemiaJ Traeger-Synodinos, A Metaxotou-Mavrommati, M Karagiorga, et al.
British Journal of Haematology|December 22, 1999
Molecular, haematological and clinical studies of the -101 C --> T substitution of the beta-globin gene promoter in 25 beta-thalassaemia intermedia patients and 45 heterozygotesE Maragoudaki, E Kanavakis, J Traeger-Synodinos, et al.
Human Genetics|May 17, 2001
CFTR gene mutations--including three novel nucleotide substitutions--and haplotype background in patients with asthma, disseminated bronchiectasis and chronic obstructive pulmonary diseaseM Tzetis, A Efthymiadou, S Strofalis, et al.
British Journal of Haematology|December 1, 1996
The triplicated alpha-globin gene locus in beta-thalassaemia heterozygotes: clinical, haematological, biosynthetic and molecular studiesJ Traeger-Synodinos, E Kanavakis, C Vrettou, et al.
Hemoglobin|June 18, 1998
An alpha-thalassemic hemoglobinopathy: homozygosity for the HB Agrinio alpha 2-globin chain variantJ Traeger-Synodinos, A Metaxotou-Mavromati, E Kanavakis, et al.
Human Genetics|September 1, 1995
Mutation analysis of ten exons of the CFTR gene in Greek cystic fibrosis patients: characterization of 74.5% of CF alleles including one novel mutationE Kanavakis, M Tzetis, T Antoniadi, et al.
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